Encapsulation film and method for encapsulating organic electronic device using same

ABSTRACT

Provided are an encapsulation film, a product for encapsulating an organic electronic device (OED) using the same, and a method of encapsulating an OED. The encapsulation film may effectively block moisture or oxygen permeating into the OED from an external environment, provide high reliability due to increases in a lifespan and durability of the OED, and minimize align errors in a process of attaching the film to a substrate.

BACKGROUND 1. Field of the Invention

The present application relates to an encapsulation film and a method ofencapsulating an organic electronic device (OED) using the same.

2. Discussion of Art

An OED is a device including an organic material layer generatingexchange of charges using holes and electrons, and may be, for example,a photovoltaic device, a rectifier, a transmitter, and an organic lightemitting diode (OLED).

An OLED among the OEDs consumes less power and has a higher responsespeed than conventional light sources, and is preferable as a thindisplay device or light. In addition, the OLED has excellent spaceutilization, and thus is expected to be applied in various fieldsincluding all kinds of portable devices, monitors, notebook computers,and TVs.

To expand commercialization and use of the OLED, the most importantproblem is durability. Organic materials and metal electrodes includedin the OLED are very easily oxidized by external factors such asmoisture. Accordingly, a product including the OLED is very sensitive toenvironmental factors. To solve the above-described problem, anencapsulant for an OED is applied. However, an automatic logisticsprocess for a thin encapsulant is difficult, and defects such as alignerrors may easily occur in a process of attaching an encapsulant to abase substrate due to a gradually-shorter bezel. Accordingly, a methodof solving the problems is needed.

SUMMARY OF THE INVENTION

The present application is directed to providing an encapsulation film,a product for encapsulating an OED using the same, and a method ofencapsulating an OED.

Hereinafter, with reference to the accompanying drawings, exemplaryembodiments of the present application will be described in furtherdetail. In addition, to explain the present application, detaileddescriptions for known general functions or configurations will beomitted. In addition, the accompanying drawings are schematicallyprovided to help in understanding the present application, and to moreclearly explain the present application, parts that do not relate to thedescriptions will be omitted, thicknesses are exaggerated to clearlyexpress several layers and regions, and the scope of the presentapplication is not limited by thicknesses, sizes, and ratios shown inthe drawings.

One aspect of the present application provides an encapsulation filmwhich may be used to attach an entire surface of an OED. Theencapsulation film includes a single-layered or multilayeredencapsulating layer including a metal layer and an encapsulating resin.

The term “organic electronic device (OED)” used herein refers to aproduct or device having a structure including an organic material layergenerating exchange of charges using holes and electrons between a pairof electrodes facing each other, and may be, but is not limited to, forexample, a photovoltaic device, a rectifier, a transmitter, and anorganic light emitting diode (OLED). In one exemplary embodiment of thepresent application, the OED may be an OLED.

According to an exemplary embodiment of the present application, theencapsulation film encapsulates an entire surface of the OED, and mayinclude a metal layer, and an encapsulating layer including anencapsulating resin and having a tensile modulus of 0.001 to 500 MPa atroom temperature.

A material for the encapsulating layer according to the presentapplication is not particularly limited as long as it satisfies therange of the tensile modulus. The tensile modulus used herein is atensile modulus measured at a temperature of 25° C. unless particularlydefined otherwise. In addition, the tensile modulus used herein mayrefer to a tensile modulus of a curable component measured after curingunless particularly defined otherwise. In one example, the tensilemodulus may refer to a tensile modulus measured after curing atapproximately 100° C. for approximately 120 minutes, a tensile modulusmeasured after radiating UV rays at a radiation dose of approximately 1J/cm² or more, or a tensile modulus measured after thermal curing isadditionally performed after UV radiation.

As described above, the encapsulating layer may have a tensile modulusof 0.001 to 500 MPa at room temperature, and for example, 0.001 to 490Mpa, 0.001 to 480 Mpa, 0.001 to 470 Mpa, 0.001 to 460 Mpa, 0.001 to 450Mpa, 0.001 to 440 Mpa, 0.001 to 430 Mpa, 0.001 to 420 Mpa, 0.001 to 410Mpa, 0.001 to 400 Mpa, 0.05 to 450 Mpa, 0.1 to 450 Mpa, 0.2 to 450 Mpa,0.3 to 450 Mpa, or 0.5 to 450 Mpa. As the tensile modulus of theencapsulating layer is controlled within a specific range, a chance tohave defects such as align errors of the encapsulation film goingthrough a process at a specific temperature may be minimized.

The metal layer according to an exemplary embodiment of the presentapplication may be transparent or opaque. A material for or a method offorming the metal layer is not particularly limited as long as itsatisfies the above-described thermal expansion coefficient range. Forexample, the metal layer may be a thin film-type metal foil, or a layerformed by depositing a metal on a polymer base substrate. The metallayer may be any one that can have thermal conductivity and moisturepreventability. The metal layer may include any one of a metal oxide, ametal nitride, a metal carbide, a metal oxynitride, a metal oxyboride,and a mixture thereof. For example, the metal layer may include a metaloxide such as silicon oxide, aluminum oxide, titanium oxide, indiumoxide, tin oxide, indium tin oxide, tantalum oxide, zirconium oxide,niobium oxide, and a mixture thereof. The metal layer may be depositedby a means for electrolysis, rolling, evaporation, electron beamevaporation, sputtering, reactive sputtering, chemical vapor deposition,plasma chemical vapor deposition, or electron cyclotron resonance sourceplasma chemical vapor deposition.

The metal layer preferably has a thermal conductivity of 50 W/mK ormore, 60 W/mK or more, 70 W/mK or more, 80 W/mK or more, 90 W/mK ormore, 100 W/mK or more, 110 W/mK or more, 120 W/mK or more, 130 W/mK ormore, 140 W/mK or more, 150 W/mK or more, 200 W/mK or more, or 250 W/mKor more. Due to the high thermal conductivity, heat generated at ajunction interface in a metal layer junction process may be more rapidlyemitted. In addition, the high thermal conductivity rapidly emits heataccumulated in operation of an OED to an external atmosphere, and thus atemperature of the OED can be maintained at a lower level, and cracksand defects can be reduced.

The metal layer according to one exemplary embodiment of the presentapplication may include a base substrate. The base substrate may be, butis not limited to, selected from polyethyleneterephthalate,polytetrafluoroethylene, polyethylene, polypropylene, polybutene,polybutadiene, a vinyl chloride copolymer, polyurethane, ethylene-vinylacetate, an ethylene-propylene copolymer, an ethylene-ethyl acrylatecopolymer, an ethylene-methyl acrylate copolymer, polyimide, nylon, anda combination thereof as a polymer resin material. The base substratemay prevent corrosion when in contact with moisture, and damage due tofolding or bending during the process.

In an exemplary embodiment of the present application, a material forthe encapsulation film is not particularly limited as long as theabove-described metal layer and the encapsulating layer are included,and a structure of the encapsulating layer is not particularly limited,either. For example, the encapsulating layer may be formed in a singlelayer or a multiple layer of at least two layers. When the encapsulatinglayer is formed in a multilayer structure, each component constitutingan encapsulating layers may be the same as or different from each other.Here, the component constituting the encapsulating layer may be anencapsulating resin, a moisture adsorbent, a curable material, or otheradditives.

In one example, the encapsulating resin may be a styrene-based resin orelastomer, a polyolefin-based resin or elastomer, other elastomers, apolyoxyalkylene-based resin or elastomer, a polyester-based resin orelastomer, a polyvinylchloride-based resin or elastomer, apolycarbonate-based resin or elastomer, a polyphenylenesulfide-basedresin or elastomer, a mixture of hydrocarbon, a polyamide-based resin orelastomer, an acrylate-based resin or elastomer, an epoxy-based resin orelastomer, a silicon-based resin or elastomer, a fluorine-based resin orelastomer, or a mixture thereof.

Here, the styrene-based resin or elastomer may be, for example, astyrene-ethylene-butadiene-styrene (SEBS) block copolymer, astyrene-isoprene-styrene (SIS) block copolymer, anacrylonitrile-butadiene-styrene (ABS) block copolymer, anacrylonitrile-styrene-acrylate (ASA) block copolymer, astyrene-butadiene-styrene (SBS) block copolymer, a styrene-basedhomopolymer, or a mixture thereof. The olefin-based resin or elastomermay be, for example, a high-density polyethylene-based resin orelastomer, a low-density polyethylene-based resin or elastomer, apolypropylene-based resin or elastomer, or a mixture thereof. Theelastomer may be, for example, an ester-based thermoplastic elastomer,an olefin-based elastomer, a silicon-based elastomer, an acryl-basedelastomer, or a mixture thereof. Among these, the olefin-basedthermoplastic elastomer may be a polybutadiene resin or elastomer or apolyisobutylene resin or elastomer. The polyoxyalkylene-based resin orelastomer may be, for example, a polyoxymethylene-based resin orelastomer, a polyoxyethylene-based resin or elastomer, or a mixturethereof. The polyester-based resin or elastomer may be, for example, apolyethylene terephthalate-based resin or elastomer, a polybutyleneterephthalate-based resin or elastomer, or a mixture thereof. Thepolyvinylchloride-based resin or elastomer may be, for example,polyvinylidene chloride. The mixture of hydrocarbon may be, for example,hexatriacotane or paraffin. The polyamide-based resin or elastomer maybe, for example, nylon. The acrylate-based resin or elastomer may be,for example, polybutyl(meth)acrylate. The epoxy-based resin or elastomermay be, for example, a bisphenol-type such as a bisphenol A-type, abisphenol F-type, a bisphenol S-type, and a hydrogenated productthereof; a novolac-type such as a phenolnovolac-type or a cresolnovolac-type; a nitrogen-containing ring-type such as atriglycidylisocyanurate-type or a hydantoin-type; an alicyclic-type; analiphatic-type; an aromatic-type such as a naphthalene-type or abiphenyl-type; a glycidyl-type such as a glycidylether-type, aglycidylamine-type, or a glycidylester-type; a dicyclo-type such as adicyclopentadiene-type; an ester-type; an etherester-type; or a mixturethereof. The silicon-based resin or elastomer may be, for example,polydimethylsiloxane. In addition, the fluorine-based rein or elastomermay be a polytrifluoroethylene resin or elastomer, apolytetrafluoroethylene resin or elastomer, apolychlorotrifluoroethylene resin or elastomer, apolyhexafluoropropylene resin or elastomer, polyvinylidene fluoride,polyvinyl fluoride, polyethylenepropylene fluoride, or a mixturethereof.

The listed resin or elastomer may be grafted with maleic anhydride,copolymerized with a monomer for preparing another listed resin orelastomer or a resin or an elastomer, and modified by another compound.The compound may be a carboxyl-terminated butadiene-acrylonitrilecopolymer.

In one exemplary embodiment, as the encapsulating resin, a copolymer ofan olefin-based compound including a carbon-carbon double bond may beincluded, but the present application is not limited.

In addition, the encapsulating resin may be a copolymer of a diene andan olefin-based compound including a carbon-carbon double bond. Here,the olefin-based compound may include isobutylene, propylene, orethylene, the diene may be a monomer that can be polymerized with theolefin-based compound, and may include, for example, 1-butene, 2-butene,isoprene, or butadiene. That is, the encapsulating resin of the presentapplication may be, for example, a homopolymer of an isobutylenemonomer; a copolymer prepared by copolymerizing a monomer that can bepolymerized with an isobutylene monomer; or a mixture thereof. In oneexample, a copolymer of an olefin-based compound including acarbon-carbon double bond and a diene may be butyl rubber.

The encapsulating resin may have a weight average molecular weight (Mw)as can be molded in the form of a film. For example, the resin may havea weight average molecular weight (Mw) of approximately 100,000 to2,000,000, 100,000 to 1,500,000, or 100,000 to 1,000,000. The term“weight average molecular weight” refers to a conversion value forstandard polystyrene measured by gel permeation chromatography (GPC).However, the resin or elastomer component may not have theabove-described weight average molecular weight. For example, when themolecular weight of the resin or elastomer component is not in asufficient level to form a film, a separate binder resin may be added toa component constituting an encapsulating layer.

In yet another embodiment, the encapsulating resin may include a curableresin. In one example, components constituting the above-describedencapsulating layer is not particularly limited as long as theencapsulating layer satisfies the tensile modulus or glass transitiontemperature, and may include, for example, a curable resin. In oneexample, the curable resin may be included as a component constituting asecond layer of the encapsulating layer, which will be described below.

A specific kind of the curable resin that can be used in the presentapplication is not particularly limited, and for example, variousheat-curable or photocurable resins known in the art may be used. The“heat-curable resin” used herein refers to a resin that can be cured bysuitable heat application or an aging process, and the term“photocurable resin” refers to a resin that can be cured by radiation ofelectromagnetic waves. In addition, here, in the category of theelectromagnetic waves, microwaves, IR rays, UV rays, X rays, γ rays. andparticle beams such as α-particle beams, proton beams, neutron beams,and electron beams may be included. In the present application, as anexample of the photocurable resin, a cationic photocurable resin may beused. The cationic photocurable resin refers to a resin that can becured by cationic polymerization or a cationic curing reaction inducedby radiation of electromagnetic waves. In addition, the curable resinmay be a dual curable resin having both heat-curable and photocurablecharacteristics.

A specific kind of a curable resin that can be used in exemplaryembodiments of the present application is not particularly limited, aslong as the curable resin has the above-described characteristics. Forexample, a resin that can be cured to exhibit adhesive characteristicsmay include a resin including at least one heat-curable functional groupselected from a glycidyl group, an isocyanate group, a hydroxyl group, acarboxyl group, or an amide group, or at least one functional groupcapable of being cured by the radiation of an electromagnetic wave,selected from an epoxide group, a cyclic ether group, a sulfide group,an acetal group, and a lactone group. In addition, a specific kind ofthe resin may include an acryl resin, a polyester resin, an isocyanateresin, or an epoxy resin, but the present application is not limitedthereto.

As the curable resin in the present application, an aromatic oraliphatic, or a linear or branched epoxy resin may be used. In oneexemplary embodiment of the present application, an epoxy resincontaining at least two functional groups and an epoxy equivalent of 180to 1,000 g/eq may be used. When the epoxy resin having the above epoxyequivalent is used, characteristics such as adhesive performance and aglass transition temperature of the cured product may be effectivelymaintained. Such an epoxy resin may be one or a mixture of at least twoof a cresol novolac epoxy resin, a bisphenol A-type epoxy resin, abisphenol A-type novolac epoxy resin, a phenol novolac epoxy resin, a4-functional epoxy resin, a biphenyl-type epoxy resin, atriphenolmethane-type epoxy resin, an alkyl-modified triphenolmethaneepoxy resin, a naphthalene-type epoxy resin, a dicyclopentadiene-typeepoxy resin, and a dicyclopentadiene-modified phenol-type epoxy resin.

In the present application, preferably, an epoxy resin including acyclic structure in a molecular structure may be used, and morepreferably, an epoxy resin including an aromatic group (for example, aphenyl group) may be used. When the epoxy resin includes an aromaticgroup, a cured product may have excellent thermal and chemicalstabilities and low moisture absorption, thereby enhancing reliabilityof the encapsulation structure of the OED. Specifically, an example ofthe epoxy resin containing an aromatic group that can be used in thepresent application may be, but is not limited to, one or a mixture ofat least two of a biphenyl-type epoxy resin, a dicyclopentadiene-typeepoxy resin, a naphthalene-type epoxy resin, adicyclopentadiene-modified phenol-type epoxy resin, a cresol-based epoxyresin, a bisphenol-based epoxy resin, a xyloc-based epoxy resin, amultifunctional epoxy resin, a phenol novolac epoxy resin, atriphenolmethane-type epoxy resin, and an alkyl-modifiedtriphenolmethane epoxy resin.

In the specification, preferably, the epoxy resin is a silane-modifiedepoxy resin, and more preferably, a silane-modified epoxy resin havingan aromatic group. Likewise, when an epoxy resin modified with a silaneto structurally have a silane group is used, an adhesive property of theOED to a glass substrate or a substrate inorganic material is maximized,and a moisture barrier property or durability and reliability may beenhanced. Such a specific kind of the epoxy resin that can be used inthe present application is not particularly limited, and the resin maybe easily obtained from a manufacturer, for example, Kukdo Chemical,Co., Ltd.

As described above, the encapsulating layer may include a single layeror a multiple layer having at least two layers. When the encapsulatinglayer is formed of a single layer, a tensile modulus of theencapsulating layer is as described above. In addition, when theencapsulating layer is formed of at least two layers, at least one layermay have a tensile modulus of 0.001 to 500 MPa at room temperature. Inaddition, when the encapsulating layer includes at least two layers, theencapsulating layer may include a first layer having a tensile modulusof 0.001 to 500 MPa at room temperature, and a second layer having atensile modulus of 500 to 1000 MPa at room temperature. When an organicelectronic diode is encapsulated with at least two layers, a stackedsequence is not particularly limited, but a layer including or notincluding a small amount of a moisture adsorbent that will be describedbelow may be in contact with the organic electronic diode.

In an exemplary embodiment of the present application, the encapsulatinglayer may further include a moisture adsorbent. The term “moistureadsorbent” may refer to any component that can adsorb or remove moistureor vapor permeating from an external environment through a physical orchemical reaction. That is, the moisture adsorbent means a moisturereactive or physical adsorbent, or a mixture thereof.

The moisture reactive adsorbent chemically reacts with vapor, moisture,or oxygen permeating into the encapsulating layer to adsorb moisture orvapor. The physical adsorbent may extend a path of moisture or vaporpermeating into the encapsulation structure to prevent the permeation,and maximize preventability to moisture and vapor through a matrixstructure of the encapsulating resin and an interaction with themoisture reactive adsorbent.

The specific kind of the moisture adsorbent that can be used in thepresent application may be, but is not particularly limited to, one or amixture of at least two of metal powder such as alumina, a metal oxide,a metal salt, or phosphorus pentoxide (P₂O₅) in the case of the moisturereactive adsorbent, and silica, zeolite, titania, zirconia, ormontmorillonite in the case of the physical adsorbent.

Here, specifically, the metal oxide may be phosphorus pentoxide (P₂O₅),lithium oxide (Li₂O), sodium oxide (Na₂O), barium oxide (BaO), calciumoxide (CaO), or magnesium oxide (MgO), and the metal salt may be, but isnot limited to, a sulfate such as lithium sulfate (Li₂SO₄), sodiumsulfate (Na)SO₄), calcium sulfate (CaSO₄), magnesium sulfate (MgSO₄),cobalt sulfate (CoSO₄), gallium sulfate (Ga₂(SO₄)₃), titanium sulfate(Ti(SO₄)₂), or nickel sulfate (NiSO₄); a metal halide such as calciumchloride (CaCl₂), magnesium chloride (MgCl₂), strontium chloride(SrCl₂), yttrium chloride (YCl₃), copper chloride (CuCl₂), cesiumfluoride (CsF), tantalum fluoride (TaF₅), niobium fluoride (NbF₅),lithium bromide (LiBr), calcium bromide (CaBr₂), cesium bromide (CeBr₃),selenium bromide (SeBr₄), vanadium bromide (VBr₃), magnesium bromide(MgBr₂), barium iodide (BaI₂), or magnesium iodide (MgI₂); or a metalchlorate such as barium perchlorate (Ba(ClO₄)₂) or magnesium perchlorate(Mg(ClO₄)₂).

In the present application, the moisture adsorbent such as the metaloxide may be suitably processed, and added to the composition. Forexample, depending on the kind of the OED to which the encapsulationfilm is applied, the encapsulating layer may be a thin film having athickness of 30 μm or less, and in this case, a grinding process of themoisture adsorbent may be needed. To grind the moisture adsorbent,three-roll milling, bead milling, or ball milling may be used. Inaddition, when the encapsulation film of the present application is usedin a top-emissive OED, a permeability of the encapsulating layer is veryimportant, and thus the moisture adsorbent should have a small size.Accordingly, for such a use, the grinding process may also be needed.

The encapsulating layer of the present application may include amoisture adsorbent at 1 to 100 parts by weight, and preferably 5 to 50parts by weight relative to 100 parts by weight of the encapsulatingresin. As the content of the moisture adsorbent is controlled to 5 partsby weight or more, the encapsulating layer may exhibit excellentmoisture and vapor preventabilities. In addition, as the content of themoisture adsorbent is controlled to 50 parts by weight or less, theencapsulating layer may be formed in a thin film having an encapsulationstructure, and exhibit excellent moisture preventability. However, thecontent range may be suitably controlled according to a location of theencapsulating layer without particular limitation. For example, themoisture adsorbent in a region of the encapsulating layer, which isclose to the OED may be included in a smaller amount, and may beincluded, for example, at 0 to 20% based on a total amount of themoisture adsorbent. When the content is more than 20%, the moistureadsorbent may induce a physical damage by pressing the OED along withimpurities, and induce a chemical damage to a negative electrode or aninorganic protective layer due to an excessive amount of ionic materialsreleased after the reaction with moisture.

In the specification, unless particularly defined otherwise, the unit“parts by weight” means a weight ratio between components.

In an exemplary embodiment of the present application, the encapsulatinglayer may further include a tackifier according to the kind of theencapsulating resin. For example, the encapsulating layer may furtherinclude a tackifier, in addition to the above-described encapsulatingresin. The tackifier may be, for example, a hydrogenated petroleum resinobtained by hydrogenating a petroleum resin. The hydrogenated petroleumresin may be partially or completely hydrogenated, and may be a mixtureof such resins. Such a tackifier may have high compatibility with acomponent constituting the encapsulating layer and an excellent moisturepreventability. The specific hydrogenated petroleum resin may be ahydrogenated terpene-based resin, a hydrogenated ester-based resin, or ahydrogenated dicyclopentadiene-based resin. The tackifier may have aweight average molecular weight of approximately 200 to 5,000. A contentof the tackifier may be suitably controlled as needed. For example, thetackifier may be included in a first layer at 5 to 100 parts by weightrelative to 100 parts by weight of the encapsulating resin.

The encapsulating layer may include various additives according to a useof the film and a process of manufacturing a film, in addition to theabove-described components. For example, in consideration of durabilityand processability, a curable material may be further included in theencapsulating layer. Here, the curable material may mean a materialhaving a heat-curable functional group and/or an active energybeam-curable functional group separately included in addition to thecomponents constituting the encapsulating layer. In addition, a contentof the curable material included in the encapsulating layer may becontrolled according to a desired physical property of the film.

In an exemplary embodiment of the present application, the encapsulatinglayer may further include a curing agent according to the kind of theencapsulating resin. For example, through a reaction with theabove-described encapsulating resin, a curing agent that can form acrosslinking structure or an initiator that can initiate a curingreaction of the resin may further be included.

A suitable kind of the curing agent may be selected and used dependingon the kind of the encapsulating resin or a functional group included inthe resin.

In one example, when the encapsulating resin is an epoxy resin, as thecuring agent, for example, a curing agent of an epoxy resin known in theart, for example, at least one or two of an amine curing agent, animidazole curing agent, a phenol curing agent, a phosphorous curingagent, and an acid anhydride curing agent may be used, but the presentapplication is not limited.

In one example, the curing agent may be an imidazole compound which is asolid at room temperature, and has a melting point or a degradationtemperature of 80° C. or more. Such a compound may be, but is notlimited to, 2-methyl imidazole, 2-heptadecyl imidazole, 2-phenylimidazole, 2-phenyl-4-methyl imidazole, or 1-cyanoethyl-2-phenylimidazole.

A content of the curing agent may be selected according to components ofthe composition, for example, a kind or ratio of the encapsulatingresin. For example, the curing agent may be included at 1 to 20 parts byweight, 1 to 10 parts by weight, or 1 to 5 parts by weight relative to100 parts by weight of the encapsulating resin. However, the weightratio may be changed according to a kind and a ratio of theencapsulating resin or a functional group of the resin, or acrosslinking density to be realized.

When the encapsulating resin is a resin that can be cured by radiationof active energy beams, as an initiator, for example, a cationicphotopolymerization initiator may be used.

As the cationic photopolymerization initiator, an onium salt ororganometallic salt-series ionized cationic initiator, or an organicsilane-series or latent sulfonic acid-series initiator, or a non-ionizedcationic photopolymerization initiator may be used. The oniumsalt-series initiator may be a diaryliodonium salt, a triarylsulfoniumsalt, or an aryldiazonium salt, the organometallic salt-series initiatormay be iron arene, the organic silane-series initiator may beo-nitrobenzyl triaryl silyl ether, triaryl silyl peroxide, or acylsilane, and the latent sulfonic acid-series initiator may beα-sulfonyloxy ketone or α-hydroxymethylbenzoin sulfonate, but thepresent application is not limited thereto.

In one example, as the cationic initiator, an ionized cationicphotopolymerization initiator may be used.

In addition, when the encapsulating resin is a resin that can be curedby radiation of active energy beams, as the initiator, for example, aradical initiator may be used.

The radical initiator may be a photoinitiator or a thermal initiator. Aspecific kind of the photoinitiator may be suitably selected inconsideration of a curing speed and yellowing probability. For example,the photoinitiator may be a benzoin-, hydroxy ketone-, amino ketone-, orphosphine oxide-based photoinitiator, and specifically, benzoin, benzoinmethylether, benzoin ethylether, benzoin isopropylether, benzoinn-butylether, benzoin isobutylether, acetophenone, dimethylaminoacetophenone, 2,2-dimethoxy-2-phenylacetophenone,2,2-diethoxy-2-phenylacetophenone,2-hydroxy-2-methyl-1-phenylpropane-1-one, 1-hydroxycyclohexylphenylketone,2-methyl-1-[4-(methylthio)phenyl]-2-morpholino-propane-1-one,4-(2-hydroxyethoxy)phenyl-2-(hydroxy-2-propyl)ketone, benzophenone,p-phenylbenzophenone, 4,4′-diethylamino benzophenone,dichlorobenzophenone, 2-methylanthraquinone, 2-ethyl anthraquinone,2-t-butylanthraquinone, 2-aminoanthraquinone, 2-methylthioxanthone,2-ethylthioxanthone, 2-chlorothioxanthone, 2,4-dimethylthioxanthone,2,4-diethylthioxanthone, benzyldimethylketal, acetophenonedimethylketal, p-dimethylamino benzoic acid ester,oligo[2-hydroxy-2-methyl-1-[4-(1-methylvinyl)phenyl]propanone], or2,4,6-trimethylbenzoyl-diphenyl-phosphineoxide.

A content of the initiator, like the curing agent, may be changedaccording to the kind and ratio of the encapsulating resin or afunctional group of the resin, or a crosslinking density to be realized.For example, the initiator may be included at 0.01 to 10 parts by weightor 0.1 to 3 parts by weight relative to 100 parts by weight of theencapsulating resin. When the content of the initiator is too small,curing may not sufficiently occur, and when the content of the initiatoris too large, a content of an ionic material is increased after curingto deteriorate durability of an adhesive, or due to the characteristicof the initiator, a conjugate acid is formed, which is disadvantageousin terms of optical durability, and corrosion may occur according to abase substrate, thereby selecting a suitable content range inconsideration of such a problem.

The encapsulating layer may include various materials according to a useof the film and a process of manufacturing a film. For example, when theencapsulating layer is molded in a film or sheet type, in considerationof moldability, a binder resin may be included in the encapsulatinglayer.

In one exemplary embodiment of the present application, theencapsulating layer may include a filler, and preferably, an inorganicfiller. The filler may extend a path of moisture or vapor permeatinginto the encapsulation structure to prevent the permeation, and maximizepreventability to moisture and vapor through an interaction with theencapsulating resin and the moisture adsorbent. A specific kind of thefiller that can be used in the present application may be, but is notparticularly limited to, for example, one or a mixture of at least twoof clay, talc, and needle-like silica.

In the present application, to increase a binding efficiency between afiller and an organic binder, as the filler, a product which issurface-treated with an organic material may be used, or a couplingagent may be further added.

The encapsulating layer of the present application may include a fillerat 1 to 50 parts by weight, and preferably 1 to 20 parts by weightrelative to 100 parts by weight of the encapsulating resin. As thecontent of the filler is controlled to 1 part by weight or more, a curedproduct having an excellent moisture or vapor blocking property andexcellent mechanical properties may be provided. In addition, in thepresent application, as the content of the filler is controlled to 50parts by weight or less, a film-type encapsulating layer can bemanufactured, and although the encapsulating layer is formed in a thinfilm, an encapsulation structure exhibiting an excellent moistureblocking characteristic may be provided.

The encapsulation film of the present application may have, but notparticularly limited, a structure including, for example, a base orreleasing film (hereinafter, can be referred to as a “first film”); andthe encapsulating layer formed on the base or releasing film as long asincluding the metal layer and the encapsulating layer.

FIGS. 1 to 2 are cross-sectional views of an encapsulation filmaccording to an exemplary embodiment of the present application.

As shown in FIG. 1, the encapsulation film of the present applicationmay include an encapsulating layer 12 and a metal layer 13 which areformed on a base or releasing film 11. In addition, in FIG. 2, theencapsulating layer 12 includes a first layer 12 a and a second layer 12b.

A specific kind of the first film that can be used in the presentapplication is not particularly limited. In the present application, asthe first film, for example, a general polymer film in the art may beused. In the present application, for example, as the base or releasingfilm, a polyethyleneterephthalate film, a polytetrafluorethylene film, apolyethylene film, a polypropylene film, a polybutene film, apolybutadiene film, a vinylchloride copolymer film, a polyurethane film,an ethylene-vinyl acetate film, an ethylene-propylene copolymer film, anethylene-acrylic acid ethyl copolymer film, an ethylene-acrylic acidmethyl copolymer film, or a polyimide film may be used. In addition, oneor both surfaces of the base or releasing film of the presentapplication may be subjected to suitable releasing treatment. As anexample of a releasing agent used in the releasing treatment of the basefilm, an alkyd-, silicon-, fluorine-, unsaturated ester-, polyolefin-,or wax-based releasing agent may be used, and among these, in terms ofheat resistance, an alkyd-, silicon-, or fluorine-based releasing agentis preferably used, but the present application is not limited thereto.

In the present application, a thickness of the base or releasing film(the first film) is not particularly limited, and may be suitablyselected according to an application. For example, in the presentapplication, the first film may have a thickness of approximately 10 to500 μm, and preferably, 20 to 200 μm. When the thickness is less than 10μm, the base film may be easily modified in the manufacturing process,and when the thickness is more than 500 μm, economic feasibility isdegraded.

The thickness of the encapsulating layer included in the encapsulationfilm of the present application is not particularly limited, and inconsideration of an application of the film, may be suitably selectedaccording to the following conditions. The thickness of theencapsulating layer may be approximately 5 to 200 μm, and preferably, 5to 100 μm. When the thickness of the encapsulating layer is less than 5μm, it may not exhibit sufficient moisture preventability, and when thethickness of the encapsulating layer is more than 200 μm, processabilityis difficult to be ensured, and thickness expansion is increased due tomoisture reactivity, thereby damaging a deposition film of the OED, anddecreasing economic feasibility.

Another aspect of the present application provides a method ofmanufacturing an encapsulation film. The exemplary encapsulation filmmay be manufactured by molding the encapsulating layer in a film orsheet type.

In one example, the method may include applying a coating solutionincluding components constituting the above-described encapsulatinglayer on a base or releasing film in a sheet or film type, and dryingthe applied coating solution.

The coating solution may be prepared by, for example, dissolving ordispersing the components of the above-described encapsulating layer ina suitable solvent. In one example, the encapsulating layer may bemanufactured by a method of dissolving or dispersing the moistureadsorbent or filler in a solvent when needed, grinding the moistureadsorbent or filler and mixing the grinded moisture adsorbent or fillerwith an encapsulating resin.

A kind of the solvent used in the preparation of a coating solution isnot particularly limited. However, when a drying time of the solvent isexcessively long, or drying at a high temperature is needed, problemsmay be generated in terms of workability or durability of theencapsulation film, and thus a solvent having a volatile temperature of150° C. or less may be used. In consideration of film moldability, asmall amount of the solvent having a volatile temperature in the rangeor more may be mixed and used. The solvent may be, but is not limitedto, at least one or two of methylethylketone (MEK), acetone, toluene,dimethylformamide (DMF), methylcellosolve (MCS), tetrahydrofuran (THF),xylene, or N-methylpyrrolidone (NMP).

A method of applying the coating solution to the base or releasing filmmay be, but is not particularly limited to, a known coating method suchas knife coating, roll coating, spray coating, gravure coating, curtaincoating, comma coating, or lip coating.

The applied coating solution may be dried, and the solvent may bevolatilized, thereby forming an encapsulating layer. The drying may beperformed, for example, at 70 to 150° C. for 1 to 10 minutes. The dryingcondition may be changed in consideration of a kind of the used solvent.

After the drying, a metal layer may be formed on the encapsulatinglayer. The metal layer may be formed using a known technique in the art.For example, the metal layer may be formed of a metal foil or bydepositing a metal on a polymer base substrate. For example, the metallayer may be formed by electrolysis or rolling.

Still another aspect of the present application provides a product forencapsulating an OED, which includes a substrate, an OED formed on thesubstrate, and the above-described encapsulation film encapsulating theOED, in which the encapsulation film is attached to an entire surface ofthe OED.

In the present application, the OED may be an OLED.

The product for encapsulating the OED may further include a protectivefilm between the encapsulation film and the OED to protect the OED.

In one example, as shown in FIG. 3, the product for encapsulating theOED may be disposed such that the encapsulating layer 12 of theencapsulation film is in contact with an OED 22 and a substrate 21. Inaddition, the metal layer 13 may be disposed on the encapsulating layer12.

Yet another aspect of the present application provides a method ofencapsulating an OED, which includes applying the above-describedencapsulating layer of the encapsulation film to a substrate on whichthe OED is formed to be attached to an entire surface of the OED, andcuring the encapsulating layer.

The encapsulation film may be applied to the OED by hot roll lamination,hot pressing, or vacuum pressing of the encapsulation film, but thepresent application is not particularly limited thereto.

In the present application, according to the method of encapsulating theOED, for example, a transparent electrode is formed on the substratesuch as a glass or a polymer film by vacuum deposition or sputtering,and an organic material layer is formed on the transparent electrode.The organic material layer may include a hole injection layer, a holetransport layer, an emitting layer, an electron injection layer, and/oran electron transport layer. Subsequently, a second electrode is furtherformed on the organic material layer. Afterward, the above-describedencapsulation film is applied to a top surface of the OED 22 on thesubstrate 21 to cover an entire surface of the OED 22. Here, a method ofapplying the encapsulation film may be, but is not particularly limitedto, a method of applying the encapsulation film of the presentapplication to a top surface of the OED 22 formed on the substrate 21through heating, pressing, or autoclaving.

In addition, an additional curing process or adhesion-enhancing processto the encapsulation film to which the OED 22 is pressed may beperformed, and such a process (main curing) may be performed, forexample, in a heating chamber. A curing condition in the main curing maybe suitably selected in consideration of stability of the OED 22.

However, the above-described forming process is merely an example forencapsulating the OED 22, and thus a sequence of or condition for theprocess may be freely changed. In addition, after the protective layeris formed on the OED 22, the encapsulation film may be applied and thencured.

Effects

An encapsulation film of the present application can effectively blockmoisture or oxygen permeating into an OED from an external environment,provide high reliability due to increases in a lifespan and durabilityof the OED, remove a process of attaching an encapsulating resin to anencap material by integrating an encap material with an encapsulatingresin, and minimize align errors in a process of attaching anencapsulation film to a substrate.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1 and 2 are cross-sectional views of an encapsulation filmaccording to an exemplary embodiment of the present application; and

FIG. 3 is a cross-sectional view of an encapsulation product of an OEDaccording to an exemplary embodiment of the present application.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

Hereinafter, the present invention will be described in further detailwith reference to Examples according to the present invention andComparative Examples not according to the present invention, but thescope of the present invention is not limited to the following Examples.

Example 1

(1) Preparation of Encapsulating Layer (First Layer)

100 g of a silane-modified epoxy resin (KSR-177, Kukdo Chemical Co.,Ltd.), 100 g of a butadiene rubber-modified epoxy resin (KR-450, KukdoChemical Co., Ltd.), and 150 g of a phenoxy resin (YP-50, Tohto KaseiCo., Ltd.) were added to a reaction vessel at room temperature, anddiluted with methylethylketone (MEK). 4 g of imidazole (ShikokuChemicals Co., Ltd.) was added as a curing agent to the homogenizedsolution, and stirred at a high speed for 1 hour, resulting in asolution for a first layer.

(2) Preparation of Encapsulating Layer (Second Layer)

A moisture adsorbent solution was prepared by adding 100 g of calcineddolomite as a moisture adsorbent and MEK having a solid content of 50 wt% as a solvent. 200 g of a silane-modified epoxy resin (KSR-177, KukdoChemical Co., Ltd.) and 150 g of a phenoxy resin (YP-50, Tohto KaseiCo., Ltd.) were added to a reaction vessel at room temperature, anddiluted with MEK. 4 g of imidazole (Shikoku Chemicals Co., Ltd.) wasadded as a curing agent to the homogenized solution, and the resultingsolution was stirred at a high speed for 1 hour, and thus a solution fora moisture barrier layer was prepared. The moisture adsorbent solutionpreviously prepared was added to the resulting solution to have acontent of the calcined dolomite of 50 parts by weight relative to 100parts by weight of an encapsulating resin of a second layer, resultingin preparing a solution for a second layer.

(3) Manufacture of Film

A second layer having a thickness of 40 μm was formed by coating thesolution for the moisture barrier layer previously prepared on areleasing surface of releasing PET, and drying the coated surface at110° C. for 10 minutes. An encapsulation film was manufactured bymanufacturing a multilayer film by laminating the first and secondlayers previously prepared, and laminating the multilayer film with a 20μm copper film.

Example 2

An encapsulation film was manufactured by the same method as describedin Example 1, except that 100 g of a silane-modified epoxy resin(KSR-177, Kukdo Chemical Co., Ltd.), 100 g of an acryl rubber-modifiedepoxy resin (KR-692, Kukdo Chemical Co., Ltd.), and 150 g of a phenoxyresin (YP-50, Tohto Kasei Co., Ltd.) were added to a reaction vessel atroom temperature and diluted with MEK, and 4 g of imidazole (ShikokuChemicals Co., Ltd.) was added as a curing agent to the homogenizedsolution and stirred at a high speed for 1 hour, resulting in a solutionfor a first layer.

Example 3

An encapsulation film was manufactured by the same method as describedin Example 1, except that 50 g of a polyisobutene resin (weight averagemolecular weight: 450,000) as an encapsulating resin of a first layerand 50 g of a hydrogenated dicyclopentadiene-based resin (softeningpoint: 125° C.) as a tackifier were added into a reaction vessel at roomtemperature, and 10 g of a DCPD-based epoxy resin and 1 g of imidazole(Shikoku Chemicals Co., Ltd.) were diluted with toluene to have a solidcontent of approximately 30 wt %.

Example 4

An encapsulation film was manufactured by the same method as describedin Example 1, except that 50 g of a polyisobutene resin (weight averagemolecular weight: 450,000) as an encapsulating resin of a crack barrierlayer and 50 g of a hydrogenated dicyclopentadiene-based resin(softening point: 125° C.) as a tackifier were added into a reactionvessel at room temperature, and 20 g of a multifunctional acryl monomer(TMPTA) and 1 g of a photoinitiator were diluted with toluene to have asolid content of approximately 25 wt %.

Example 5

A moisture adsorbent solution was prepared by adding 100 g of calcineddolomite as a moisture adsorbent and toluene as a solvent to have asolid content of 50 wt %. An encapsulation film was manufactured by thesame method as described in Example 1, except that 50 g of apolyisobutene resin (weight average molecular weight: 450,000) as anencapsulating resin of a first layer and 50 g of a hydrogenateddicyclopentadiene-based resin (softening point: 125° C.) as a tackifierwere added into a reaction vessel at room temperature, and 10 g of amultifunctional acryl monomer (TMPTA) and 1 g of a photoinitiator werediluted with toluene to have a solid content of approximately 25 wt %,and a second layer was excluded.

Example 6

An encapsulation film was manufactured by laminating the encapsulatinglayer formed in the first layer of Example 5 on an aluminum film.

Comparative Example 1

An encapsulation film was manufactured by the same method as describedin Example 1, except that 200 g of a silane-modified epoxy resin(KSR-177, Kukdo Chemical Co., Ltd.) and 150 g of a phenoxy resin (YP-50,Tohto Kasei Co., Ltd.) were added to a reaction vessel at roomtemperature, and diluted with MEK, and a solution for a first layer wasprepared by adding 4 g of imidazole (Shikoku Chemicals Co., Ltd.) as acuring agent to the homogenized solution, and stirring the resultingsolution at a high speed for 1 hour.

Comparative Example 2

An encapsulation film was manufactured by the same method as describedin Example 1, except that an encapsulating layer formed of only thesecond layer of Example 1 was used.

1. Measurement of Tensile Modulus

A coating film having a thickness of 40 μm was formed by laminating thecrack barrier layer or moisture barrier layer manufactured in Example orComparative Example. A sample was prepared by cutting the manufacturedcoating film to a size of 50 mm×10 mm (length×width) by setting acoating direction in the manufacture to a length direction, and bothsides of the sample were taped to only have a length of 25 mm.Subsequently, the taped parts were extended at a speed of 18 mm/min at25° C., and a tensile modulus was measured.

2. Measurement of Warpage in Evaluation of High Temperature and HighHumidity Reliability

A sample was manufactured by laminating the film manufactured in Exampleor Comparative Example on a cover substrate, laminating the resultingsubstrate between glass substrates, and pressured and thermal pressingthe resulting product at 70° C. Afterward, the sample was maintained ina constant temperature and constant humidity chamber at 85° C. and arelative humidity of 85% for approximately 300 hours. When warpageoccurred, it was represented as X, and when warpage did not occur, itwas represented as O.

TABLE 1 Adhesion failure in evaluation of high temperature and Tensilemodulus Tensile modulus high humidity of second layer of first layerreliability Example 1 650 MPa 400 MPa ◯ Example 2 900 MPa 450 MPa ◯Example 3 900 MPa 100 MPa ◯ Example 4 900 MPa  10 MPa ◯ Example 5 —  10MPa ◯ Example 6 —  10 MPa ◯ Comparative  1 GPa 900 MPa X Example 1Comparative 900 MPa — X Example 2

DESCRIPTION OF REFERENCE NUMERALS

-   -   11: base or releasing film    -   12: encapsulating layer        -   12 a: a first layer        -   12 b: a second layer    -   13: metal layer    -   21: substrate    -   22: organic electronic device

1. An encapsulation film for encapsulating an organic electronic device,comprising: a metal layer; and an encapsulating layer comprising anencapsulating resin, and having a tensile modulus of 0.001 to 500 MPa atroom temperature.
 2. The film according to claim 1, wherein the metallayer has a thermal conductivity of 50 W/mK or more.
 3. The filmaccording to claim 1, wherein the metal layer comprises any one of ametal oxide, a metal nitride, a metal carbide, a metal oxynitride, ametal oxyboride, and a mixture thereof.
 4. The film according to claim3, wherein the metal layer comprises any one of silicon oxide, aluminumoxide, titanium oxide, indium oxide, tin oxide, indium tin oxide,tantalum oxide, zirconium oxide, niobium oxide, and a mixture thereof.5. The film according to claim 1, wherein the metal layer furthercomprises a base substrate.
 6. The film according to claim 5, whereinthe base substrate is any one of polyethyleneterephthalate,polytetrafluoroethylene, polyethylene, polypropylene, polybutene,polybutadiene, a vinyl chloride copolymer, polyurethane, ethylene-vinylacetate, an ethylene-propylene copolymer, an ethylene-ethyl acrylatecopolymer, an ethylene-methyl acrylate copolymer, polyimide, nylon, anda combination thereof.
 7. The film according to claim 1, wherein theencapsulating layer is formed in a single layer or at least two layers.8. The film according to claim 7, wherein when the encapsulating layeris formed in at least two layers, at least one layer has a tensilemodulus of 0.001 to 500 MPa at room temperature.
 9. The film accordingto claim 1, wherein the encapsulating resin is a styrene-based resin, apolyolefin-based resin, a thermoplastic elastomer, apolyoxyalkylene-based resin, a polyester-based resin, apolyvinylchloride-based resin, a polycarbonate-based resin, apolyphenylenesulfide-based resin, a mixture of hydrocarbon, apolyamide-based resin, an acrylate-based resin, an epoxy-based resin, asilicon-based resin, a fluorine-based resin, or a mixture thereof. 10.The film according to claim 1, wherein the encapsulating resin comprisesa curable resin.
 11. The film according to claim 10, wherein the curableresin comprises at least one curable functional group selected from aglycidyl group, an isocyanate group, a hydroxyl group, a carboxyl group,an amide group, an epoxide group, a cyclic ether group, a sulfide group,an acetal group, and a lactone group.
 12. The film according to claim10, wherein the curable resin is an epoxy resin comprising a cyclicstructure in a molecular structure.
 13. The film according to claim 10,wherein the curable resin is a silane-modified epoxy resin.
 14. The filmaccording to claim 1, wherein the encapsulating layer further comprisesa moisture adsorbent.
 15. A product for encapsulating an organicelectronic device, comprising: a substrate; an organic electronic deviceformed on the substrate; and the encapsulation film according to claim 1to encapsulate the organic electronic device, wherein an encapsulatinglayer of the encapsulation film is attached to an entire surface of theorganic electronic device.
 16. The product according to claim 15,wherein the organic electronic device is an organic light emittingdiode.
 17. A method of encapsulating an organic electronic device,comprising: applying an encapsulating layer of the encapsulation filmaccording to claim 1 to a substrate on which an organic electronicdevice is formed to be attached to an entire surface of the organicelectronic device; and curing the encapsulating layer.